2,4,6-TRICHLOROANISOLE

87-40-1

1,3,5-Trichloro-2-methoxybenzene

Tyrene

2,4,6-Trichloro-1-methoxybenzene

TRICHLOROANISOLE

Benzene, 1,3,5-trichloro-2-methoxy-

Methyl 2,4,6-trichlorophenyl ether

Anisole, 2,4,6-trichloro-

2,4.6-Trichloroanisole

1,3,5-trichloro-2-methoxy-benzene

MFCD00000588

NSC-35142

31O3X41254

UNII-31O3X41254

EINECS 201-743-5

NSC 35142

2,6-Trichloroanisole

AI3-09173

Anisole,4,6-trichloro-

2,4,6-Trichloro-Anisole

SCHEMBL54507

1,5-Trichloro-2-methoxybenzene

DTXSID9073886

CHEBI:19333

2,4,6-Trichloroanisole, 99%

Methyl 2,6-trichlorophenyl ether

Benzene,3,5-trichloro-2-methoxy-

NSC35142

AKOS015849927

Anisole, 2,4,6-trichloro- (8CI)

2,4,6-TRICHLOROANISOLE [MI]

1,3,5-Trichloro-2-methoxybenzene, 9CI

AS-60959

SY051443

1-METHOXY-2,4,6-TRICHLOROBENZENE

DB-057000

CS-0150571

NS00008077

T0867

Benzene, 1,3,5-trichloro-2-methoxy- (9CI)

F20912

Q209191

2,4,6-Trichloroanisole 10 microg/mL in Isooctane

2,4,6-Trichloroanisole 100 microg/mL in Methanol

2,4,6-Trichloroanisole 1000 microg/mL in Methanol

2,4,6-Trichloroanisole, PESTANAL(R), analytical standard

InChI=1/C7H5Cl3O/c1-11-7-5(9)2-4(8)3-6(7)10/h2-3H,1H

Methyl butyrate

Methyl butanoate

623-42-7

Butanoic acid, methyl ester

METHYL N-BUTYRATE

Butyric acid, methyl ester

Methyl n-butanoate

Methyl-n-butyrate

n-Butyric acid methyl ester

FEMA No. 2693

Butyric acid methyl ester

Methyl butyrate (natural)

NSC 9380

HSDB 5721

Butanoic acid methyl ester

EINECS 210-792-1

UNII-CGX598508O

BRN 1740743

DTXSID5047083

AI3-06009

CGX598508O

NSC-9380

Methyl ester of butanoic acid

DTXCID3027083

CHEBI:88806

4-02-00-00786 (Beilstein Handbook Reference)

MFCD00009391

WE(1:0/4:0)

UN1237

Methyl butyrate, 99%

methanol I ethyl acetate

methanol - ethyl acetate

methyl 3-methylpropionate

Butyric acid-methyl ester

METHYL-N-BUTANOATE

n-C3H7COOCH3

C04 FAME

SCHEMBL13685

METHYL BUTYRATE [MI]

WLN: 3VO1

CHEMBL15859

METHYL BUTYRATE [FCC]

BUTYRIC ACID METHYLESTER

METHYL BUTYRATE [FHFI]

Methyl butyrate, >=98%, FG

METHYL N-BUTYRATE [HSDB]

NSC9380

Methyl butyrate, analytical standard

Tox21_301821

LMFA07010528

N-BUTYRIC ACID, METHYL ESTER

AKOS008907317

MCULE-1092030267

UN 1237

Methyl butyrate, natural, >=98%, FG

NCGC00256040-01

CAS-623-42-7

LS-13072

DB-054136

B0763

NS00012861

EN300-70279

n-Butyric acid methyl ester [standard material]

Methyl butyrate [UN1237] [Flammable liquid]

Q420701

J-522595

5ADC8486-F8C0-4A7A-ACD5-2234D52DE6E0

4-Methylumbelliferyl-N-acetyl-beta-D-galactosaminidehydrate

Methyl butyrate, certified reference material, TraceCERT(R)

InChI=1/C5H10O2/c1-3-4-5(6)7-2/h3-4H2,1-2H

The Henry's Law constant for methyl n-butyrate is 2.05X10-4 atm-cu m/mole(1). This Henry's Law constant indicates that methyl n-butyrate is expected to volatilize from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 4 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 5 days(SRC). Methyl n-butyrate's Henry's Law constant(1) indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of methyl n-butyrate from dry soil surfaces may exist(SRC) based upon a vapor pressure of 32.3 mm Hg(3).
Literature: (1) Buttery RG et al; J Agric Food Chem 17: 385-89 (1969) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Yaws CL; Handbook of Vapor Pressure. Vol 2 C5-C7 Compounds. Houston, TX: Gulf Pub Co (1994)

The Koc of methyl n-butyrate is estimated as 120(SRC), using a log Kow of 1.29(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that methyl n-butyrate is expected to have high mobility in soil(SRC).
Literature: (1) Hansch C et al; Exploring QSAR. Hydrophobic, Electronic, and Steric Constants. ACS Prof Ref Book. Heller SR, consult. ed., Washington, DC: Amer Chem Soc p. 14 (1995) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 4-9 (1990) (3) Swann RL et al; Res Rev 85: 17-28 (1983)

Methyl 2-methylpentanoate

2177-77-7

Methyl 2-methylvalerate

2-Methylpentanoic acid methyl ester

Valeric acid, 2-methyl-, methyl ester

Pentanoic acid, 2-methyl-, methyl ester

FEMA No. 3707

2-Methylvaleric acid, methyl ester

25KKE63345

2-Methylvaleric acid methyl ester

methyl 2-methyl valerate

Methyl 2-methylpentanoate #

SCHEMBL184608

methylpentanoic acid methyl ester

UNII-25KKE63345

FEMA 3707

DTXSID90862856

CHEBI:179995

?METHYL 2-METHYLPENTANOATE

Methyl (+/-)-2-methylpentanoate

EINECS 218-543-9

Methyl 2-methylpentanoate, >=98%

LMFA07010942

MFCD00036653

AKOS009157922

METHYL 2-METHYLPENTANOATE [FHFI]

(+/-)-METHYL 2-METHYLPENTANOATE

AS-77423

AI3-28502

DB-045694

CS-0449632

METHYL 2-METHYLPENTANOATE, (+/-)-

NS00049964

D92993

.ALPHA.-METHYLPENTANOIC ACID METHYL ESTER

Q27253977

Methyl 3-methylpentanoate

2177-78-8

Methyl 3-methylvalerate

METHYL3-METHYLPENTANOATE

Valeric acid, 3-methyl-, methyl ester

Pentanoic acid, 3-methyl-, methyl ester

Pentanoic acid,3-methyl-,methyl ester

methyl-3-methyl pentanoate

Methyl .beta.-methylvalerate

SCHEMBL5711131

DTXSID70334182

3-Methylvaleric acid, methyl ester

Methyl 3-methylvalerate, >=97.0%

DB-066628

J-014282

2,2-[1,4-PHENYLENEBIS(METHYLENE)]BIS-1H-BENZOIMIDAZOLE

3-Octanone

Octan-3-one

106-68-3

Ethyl amyl ketone

Ethyl pentyl ketone

Amyl ethyl ketone

n-Octanone-3

Ethyl n-pentyl ketone

Ethyl n-amyl ketone

3-Oxooctane

3-Octanone (natural)

FEMA No. 2803

Ethyl n-amylketone

n-AMYL ETHYL KETONE

NSC 60161

HSDB 5371

EAK

EINECS 203-423-0

BRN 1700021

CCRIS 8808

DTXSID3041954

CHEBI:80946

AI3-36116

NSC-60161

UNII-79173B4107

OCTANONE, 3-

DTXCID1021954

MFCD00009515

79173B4107

2-Heptanone, methyl-

UN2271

1-ethyl hexanal

3-octanon

octane-3-one

octan-6-one

3-OCTANONE [MI]

3-Octanone, >=98%

SCHEMBL5593

3-OCTANONE [FHFI]

3-OCTANONE [HSDB]

Ethyl amyl ketone [UN2271] [Flammable liquid]

WLN: 5V2

3-Octanone, analytical standard

3-Octanone, >=98%, FG

CHEMBL2269087

FEMA 2803

NSC60161

Tox21_301208

BBL011431

LMFA12000055

STL146538

AKOS005720776

MCULE-2012071553

NCGC00248338-01

NCGC00255105-01

CAS-106-68-3

VS-02948

3-Octanone, natural (US), >=97%, FG

NS00011968

O0122

C17145

EN300-396111

A801482

Ethyl amyl ketone [UN2271] [Flammable liquid]

J-001627

Q18349104

106-68-3(3-octanone); 541-85-5(5-methyl-3-heptanone)

The Henry's Law constant for 3-octanone is estimated as 1.3X10-4 atm-cu m/mole(SRC) derived from its vapor pressure, 2.0 mm Hg(1), and water solubility, 2600 mg/L(1). This Henry's Law constant indicates that 3-octanone is expected to volatilize from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 11 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 6.8 days(SRC). 3-Octanone's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of 3-octanone from dry soil surfaces may exist based upon its vapor pressure(1).
Literature: (1) Lande SS et al; Investigation of Selected Potential Environmental Contaminants: Ketonic Solvents. USEPA-560/2-76-003. Washington, DC: USEPA, Office of Toxic Substances (1976) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)

The Koc of 3-octanone is estimated as 58(SRC), using a water solubility of 2600 mg/L(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that 3-octanone is expected to have high mobility in soil.
Literature: (1) Lande SS et al; Investigation of Selected Potential Environmental Contaminants: Ketonic Solvents. USEPA-560/2-76-003. Washington, DC: USEPA, Office of Toxic Substances (1976) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 4-9 (1990) (3) Swann RL et al; Res Rev 85: 17-28 (1983)